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Characterization of Immune Cell Subset Expansion in Response to Therapeutic Treatment in Mice
J. Tomala, JB. Spangler
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
- MeSH
- analýza jednotlivých buněk metody MeSH
- CD4-pozitivní T-lymfocyty transplantace MeSH
- CD8-pozitivní T-lymfocyty transplantace MeSH
- imunofenotypizace MeSH
- myši transgenní MeSH
- myši MeSH
- nádory imunologie terapie MeSH
- ovalbumin aplikace a dávkování imunologie MeSH
- převzatá imunita MeSH
- průběh práce MeSH
- průtoková cytometrie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Flow cytometry has revolutionized the field of molecular immunology, enabling the monitoring and characterization of immune events at the single-cell level. Here, we describe a flow cytometry-based workflow to quantify the activation of specific immune cell subsets in mice in response to a molecular intervention. Compared to laborious long-term disease models, this technique allows for relatively rapid evaluation of candidate therapeutics designed to elicit a targeted immune response. This approach has the range to address both disease applications in which an immunostimulatory effect would be desired (e.g., cancer, infectious disease) or those in which an immunosuppressive effect would be desired (e.g., autoimmune disorders, transplantation medicine). Overall, our technique presents a powerful and accessible strategy for preliminary in vivo assessment of potential immunotherapeutics.
Department of Biomedical Engineering Johns Hopkins University Baltimore MD USA
Department of Chemical and Biomolecular Engineering Johns Hopkins University Baltimore MD USA
Institute of Microbiology of the Czech Academy of Sciences Prague Czech Republic
Citace poskytuje Crossref.org
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- $a Flow cytometry has revolutionized the field of molecular immunology, enabling the monitoring and characterization of immune events at the single-cell level. Here, we describe a flow cytometry-based workflow to quantify the activation of specific immune cell subsets in mice in response to a molecular intervention. Compared to laborious long-term disease models, this technique allows for relatively rapid evaluation of candidate therapeutics designed to elicit a targeted immune response. This approach has the range to address both disease applications in which an immunostimulatory effect would be desired (e.g., cancer, infectious disease) or those in which an immunosuppressive effect would be desired (e.g., autoimmune disorders, transplantation medicine). Overall, our technique presents a powerful and accessible strategy for preliminary in vivo assessment of potential immunotherapeutics.
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